Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
-/TT/TTT|MAF: 0.44 (TT)
Location

Chromosome 10: between 62389439 and 62389440 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2510 sample genotypes.

Variant displays